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LAClotion
LAClotion - 0574-2021-08 - (Ammonium Lactate)
Drug Information of LAClotion
| Product NDC: | 0574-2021 |
| Proprietary Name: | LAClotion |
| Non Proprietary Name: | Ammonium Lactate |
| Active Ingredient(s): | 120 mg/g & nbsp; Ammonium Lactate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LAClotion
| Product NDC: | 0574-2021 |
| Labeler Name: | Paddock Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075575 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020611 |
Package Information of LAClotion
| Package NDC: | 0574-2021-08 |
| Package Description: | 225 g in 1 BOTTLE, PLASTIC (0574-2021-08) |
NDC Information of LAClotion
| NDC Code | 0574-2021-08 |
| Proprietary Name | LAClotion |
| Package Description | 225 g in 1 BOTTLE, PLASTIC (0574-2021-08) |
| Product NDC | 0574-2021 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ammonium Lactate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20020611 |
| Marketing Category Name | ANDA |
| Labeler Name | Paddock Laboratories, Inc. |
| Substance Name | AMMONIUM LACTATE |
| Strength Number | 120 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
